HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482258Generated: October 26, 2026
Sodium hydride → 3-Methyl-7-(methylpivaloyl)xanthine
https://huagongshe.com/reaction/482258
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Methylxanthine | HCID 70639 | — |
| Reactant | 1-(5-Ketohexyl)-3-methylxanthine | HCID 15023898 | — |
| Reactant | 4-Chloro-2,2-dimethylbutanoate | HCID 21753047 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Methyl-7-(methylpivaloyl)xanthine | HCID 21584233 | 90% |
Reaction Steps
This example illustrates a method for synthesis of CT1505 (1-(5-oxohexyl)-3-methylxanthine). A mixture of 3-methylxanthine (1.00 g, 6.0 mmol) and NaH (145 mg, 6.0 mmol) in DMSO (dimethyl sulfoxide) (20 ml) was stirred until homogeneous (about 30 min). Chloromethylpivalate (865 μl, 904 mg, 6.0 mmol) was added and the reaction mixture was stirred for 18 hrs. The reaction mixture was poured into 70 ml of water and extracted with 25% ethanol/dichloromethane (4×60 ml). The combined organic extracts were combined, dried with sodium sulfate, and then evaporated in a rotoevaporator to a volume of 40 ml. The solution was cooled in ice water and it formed a thick, white precipitate. The solid was filtered off under suction and dried under vacuum to give the 3-methyl-7-(methylpivaloyl)xanthine (1.43 g, 5.4 mmol, 90% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05795897 |
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| Source dataset | uspto-grants-1998_08 |
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| ORD ID | ord-c0b5bd0b04e8470b9dc18c6a16097b15 |
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| Source note | uspto-grants-1998_08 |
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